Adipose tissue dynamics, thermogenesis, and interorgan connections for preventing obesity and metabolic disorders
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DOI[10.31662/jmaj.2023-0218]のデータに遷移します
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- 資料種別
- 記事
- 著者・編者
- Masaji Sakaguchi
- 出版年月日等
- 2024-04-15
- 出版年(W3CDTF)
- 2024-04-15
- タイトル(掲載誌)
- JMA Journal
- 巻号年月日等(掲載誌)
- 7(2)
- 掲載巻
- 7(2)
- ISSN(掲載誌)
- 2433-3298
- ISSN-L(掲載誌)
- 2433-328X
- 本文の言語コード
- eng
- DOI
- 10.31662/jmaj.2023-0218
- 国立国会図書館永続的識別子
- info:ndljp/pid/14495111
- コレクション(共通)
- コレクション(障害者向け資料:レベル1)
- コレクション(個別)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- 収集根拠
- インターネット資料収集保存事業(WARP)
- 受理日(W3CDTF)
- 2025-10-21T09:04:40+09:00
- 保存日(W3CDTF)
- 2024-09-26
- 記録形式(IMT)
- application/pdf
- オンライン閲覧公開範囲
- インターネット公開
- 遠隔複写可否(NDL)
- 不可
- 掲載誌(国立国会図書館永続的識別子)
- info:ndljp/pid/14495108
- 連携機関・データベース
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- 要約等
- <p>Adipose tissues, such as white, brown, and beige tissues, play pivotal roles in maintaining energy balance and metabolic health. Whereas white adipocytes store energy, brown and beige adipocytes exhibit high energy expenditure owing to their distinct mitochondrial density and UCP1 expression. Dysfunction in these tissues contributes to metabolic disorders such as type 2 diabetes and cardiovascular diseases. Adipose tissue expansion through cell enlargement or increased cell numbers caused by excess energy storage in white adipocytes substantially influences metabolic health. In obesity, hypertrophic adipocytes trigger inflammation, fibrosis, and hypoxia, whereas smaller adipocytes exert favorable metabolic effects, contributing to insulin sensitivity.</p><p>Brown and beige adipocytes consume energy for thermogenesis to maintain body temperature, contributing to metabolic homeostasis. The intricate interactions between brown adipose tissues and various organs, such as the liver and heart, highlight the systemic implications of adipose tissue functions. Understanding the complex underlying mechanisms may lead to the development of innovative therapies targeting metabolic disorders by modulating the functions of brown adipose tissue and its interactions with other physiological systems. In this review, we discuss insights into the mechanisms underlying the dysregulation of metabolism owing to abnormalities in adipose tissue remodeling. We focus on the endocrine functions of thermogenic brown and beige adipocytes and explore the interorgan interactions that influence whole-body metabolism.</p>
- DOI
- 10.31662/jmaj.2023-0218
- オンライン閲覧公開範囲
- インターネット公開
- 連携機関・データベース
- 科学技術振興機構 : J-STAGE
- 要約等
- <p>Adipose tissues, such as white, brown, and beige tissues, play pivotal roles in maintaining energy balance and metabolic health. Whereas white adipocytes store energy, brown and beige adipocytes exhibit high energy expenditure owing to their distinct mitochondrial density and UCP1 expression. Dysfunction in these tissues contributes to metabolic disorders such as type 2 diabetes and cardiovascular diseases. Adipose tissue expansion through cell enlargement or increased cell numbers caused by excess energy storage in white adipocytes substantially influences metabolic health. In obesity, hypertrophic adipocytes trigger inflammation, fibrosis, and hypoxia, whereas smaller adipocytes exert favorable metabolic effects, contributing to insulin sensitivity.</p><p>Brown and beige adipocytes consume energy for thermogenesis to maintain body temperature, contributing to metabolic homeostasis. The intricate interactions between brown adipose tissues and various organs, such as the liver and heart, highlight the systemic implications of adipose tissue functions. Understanding the complex underlying mechanisms may lead to the development of innovative therapies targeting metabolic disorders by modulating the functions of brown adipose tissue and its interactions with other physiological systems. In this review, we discuss insights into the mechanisms underlying the dysregulation of metabolism owing to abnormalities in adipose tissue remodeling. We focus on the endocrine functions of thermogenic brown and beige adipocytes and explore the interorgan interactions that influence whole-body metabolism.</p>
- DOI
- 10.31662/jmaj.2023-0218
- オンライン閲覧公開範囲
- インターネット公開
- 関連情報(URI)
- 連携機関・データベース
- 国立情報学研究所 : CiNii Research
- 提供元機関・データベース
- Japan Link Center雑誌記事索引データベースCrossref
- 書誌ID(NDLBibID)
- 14495111